Search

Author/Creator Howe, Jennifer

2. Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testing. Issue 11 (20th October 2021)

Authors:
Peltekova, Iskra; Yusuf, Afiqah; Frei, Jennifer; Savion‐Lemieux, Tal; Joober, Ridha; Howe, Jennifer; Scherer, Stephen W.; Elsabbagh, Mayada
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 11(2021)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. INZ‐701 Prevents Ectopic Tissue Calcification and Restores Bone Architecture and Growth in ENPP1‐Deficient Mice. (5th May 2021)

Authors:
Cheng, Zhiliang; O'Brien, Kevin; Howe, Jennifer; Sullivan, Caitlin; Schrier, Denis; Lynch, Angela; Jungles, Steven; Sabbagh, Yves; Thompson, David
Journal:
Journal of bone and mineral research
Issue:
Volume 36:Number 8(2021)
Page Start:
1594
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. MO751: Calciphylaxis is Characterized by Pyrophosphate Deficiency in Dialysis Patients: A Pilot Study. (3rd May 2022)

Authors:
Nigwekar, Sagar; St Hillien, Shelsea; Seethapathy, Rituvanthikaa; Krinsky, Scott; Torcatti, Jeanfranco; Howe, Jennifer; Kalim, Sahir; Portales-Castillo, Ignacio; Mengesha, Beza; Wen, Wen; Cizman, Borut; Sabbagh, Yves
Journal:
Nephrology dialysis transplantation
Issue:
Volume 37(2022)Supplement 3
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. INZ‐701, a recombinant ENPP1 enzyme, prevents ectopic calcification in an Abcc6−/− mouse model of pseudoxanthoma elasticum. Issue 7 (16th May 2022)

Authors:
Jacobs, Ida Joely; Cheng, Zhiliang; Ralph, Douglas; O'Brien, Kevin; Flaman, Lisa; Howe, Jennifer; Thompson, David; Uitto, Jouni; Li, Qiaoli; Sabbagh, Yves
Journal:
Experimental dermatology
Issue:
Volume 31:Issue 7(2022)
Page Start:
1095
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm gene. Issue 4 (20th January 2021)

Authors:
Hoang, Ny; Yuen, Ryan K.C.; Howe, Jennifer; Drmic, Irene; Ambrozewicz, Patricia; Russell, Carolyn; Vorstman, Jacob; Weiss, Shelly K.; Anagnostou, Evdokia; Malow, Beth A.; Scherer, Stephen W.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 4(2021)
Page Start:
1120
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗